Canonical Allele Identifier: PA645381255
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 418018
ClinVar RCV Id: RCV000482506 RCV000677488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Glu483Asp
CA16618212
NM_000046.5:c.1449A>T
CA360339088
NM_000046.5:c.1449A>C